Safety needle assembly

ABSTRACT

The present invention is directed to a safety needle assembly having the high safety and high operability, comprising: a hub; a cannula; a collar; a protector; and a sheath. The sheath includes an opening of housing the cannula; a cannula fixing part of locking the cannula housed in the opening; an attachment part of rotatably supporting the sheath attached to the hub or the collar; and a protrusive stopper which a user pushes by a finger to pivot the sheath thereby to house the cannula in the opening of the sheath. Herein, the stopper is arranged at a vicinity of a central portion of the sheath in a longitudinal direction at the opposite side of the aperture of the opening, or arranged at a portion closer to a distal end side than the central portion of the sheath.

BACKGROUND OF THE INVENTION

Field of the Invention

The present invention relates to a needle assembly having a safetymechanism (that is, comprised of a needle and attachment parts).

Description of the Related Art

Conventionally, different types of needles such as needles for ahypodermic syringe and a catheter have been applied to a medical tool.Here, a user (such as a health care worker) has to safely handle thoseneedles. Otherwise, if a user erroneously sticks such a needle used fora patient or the like into the user's own body (finger or the like), theuser may be infected with a disease.

Herein, there may be a method for preventing such a sting accident fromhappening, for example, including a means of covering a used needle witha cylindrical cap. However, even in this method, a user may erroneouslystick a needle into one of user's fingers holding the cap. Therefore,this method cannot be perfectly safe for preventing a sting accident.

Regarding other methods, for example, Patent Documents 1 and 2 disclosea technique for preventing a sting accident by using a needle assemblycomprised of a sheath (or shield) for covering a needle. According tothat technique, a user can utilize the needle assembly in the steps of:using a needle for a medical treatment; pivoting a sheath by finger(s)so as to cover the used needle with the sheath; and fixing the statethat the used needle is covered by the sheath.

PRIOR ART DOCUMENTS Patent Documents

Patent Document 1: JP 2000-140109

Patent Document 2: JP 2005-525198

However, it should be noted that the technique disclosed in PatentDocument 1 needs large force for using the needle assembly, since thereis only a short distance between a fulcrum of the pivoting sheath and aposition on the sheath which a user pushes by a finger. This results inthe poor operability of the needle assembly.

Further, according to a technique disclosed in Patent Document 2, nostopper which a user pushes by a finger to pivot a sheath is providedwith the needle assembly. This also results in the poor operability ofthe needle assembly.

Accordingly, from the viewpoint of the above mentioned drawbacks, thepresent invention has been developed so as to provide a safety needleassembly having the high safety and operability.

MEANS FOR SOLVING THE PROBLEMS

The present invention is directed to a safety needle assembly includinga sheath having the following features. That is, the sheath comprises: ahub including a proximal end connecting with a syringe, and a distalend; a cannula having a proximal end connecting with the distal end ofthe hub, a lumen extending in a longitudinal direction of the cannula,and a distal end; a collar attached to the hub and having a sheathattachment part; a protector covering the distal end of the cannula bybeing attached to the hub or the collar, and being detachable to exposethe distal end of the cannula; an opening partially extending along atleast a longitudinal direction of the sheath so as to house the cannula.

The sheath further comprises: a cannula fixing part of locking thecannula housed in the opening; an attachment part rotatably supportingthe sheath in a direction of housing the cannula when the protector isdetached to expose the distal end of the cannula, the attachment partbeing attached to the sheath attachment part of the collar; and aprotrusive stopper arranged at a vicinity of a central portion of thesheath in a longitudinal direction in which the central portion islocated at an opposite side of an aperture of the opening, or arrangedat a position closer to the distal end of the sheath than the centralportion. Herein, a user's finger pushes the stopper on the sheath so asto house the cannula in the opening.

The above mentioned mechanism allows the safety needle assembly torealize the high safety. Further, the sheath provided with theprotrusive stopper arranged at a vicinity of a central portion of thesheath in a longitudinal direction, or arranged at a position closer tothe distal end of the sheath than the central portion also allows thesafety needle assembly to realize the high operability.

More specifically, the stopper located at the position as describedabove enables the user to push the stopper on the sheath by a finger ata far position from the fulcrum, allowing a large moment to begenerated. This large moment enables the sheath to be pivoted byrelatively small force.

Further, the present invention is also directed to a safety needleassembly including a sheath having the following features. That is, thesheath comprises: a hub including a proximal end connecting with asyringe and a distal end; a cannula having a proximal end connectingwith the distal end of the hub, a lumen extending in a longitudinaldirection, and a distal end; a collar attached to the hub and having asheath attachment part and a pair of sheath fixing protrusions; aprotector covering the distal end of the cannula by being attached tothe hub or the collar, and being detachable to expose the distal end ofthe cannula; and an opening partially extending along at least alongitudinal direction of the sheath so as to house the cannula.

The sheath further comprises: a cannula fixing part comprised of groovesrespectively fitting with the pair of sheath fixing protrusions when thecannula is housed in the opening, and a pair of wing walls each of whichhas a slope arranged inside the wall in a direction from the groove tothe proximal end of the sheath; and an attachment part rotatablysupporting the sheath in a direction of housing the cannula when theprotector is detached to expose the distal end of the cannula, theattachment part being attached to the sheath attachment part of thecollar.

The above mentioned mechanism allows the safety needle assembly torealize the high safety. Further, the sheath provided with the pair ofwing walls including the grooves and slopes allows the safety needleassembly to realize the high operability. More specifically, the wingwall protruding from the sheath body has flexibility to be easily bendedoutside. Further, the slopes allow the sheath fixing protrusions locatedon the collar to be more easily introduced into the grooves. Moreover,the grooves facilitate the sheath fixing protrusions of the collar to befixed with the sheath.

Accordingly, this construction enables the sheath fixing protrusionslocated on the collar to be fitted and fixed to the gloves in the wingwalls of the sheath, by relatively small force when a user pushes thesheath by a finger.

Further, in the present invention, preferably the sheath comprises acircular recess, and a slope having a plurality of protrusions andrecesses with large frictional resistance arranged between the circularrecess and the stopper. Herein, the circular recess and the slope areused as a finger guiding region to which a user's finger of operatingthe sheath contacts, and arranged at a position closer to a proximal endside than the stopper arranged at the opposite side of the aperture ofthe opening.

The above mentioned construction enables the user to push the sheath ateither of the positions at: the circular recess to which a user's fingereasily fits, or the slope having a plurality of protrusions and recesseswith large friction resistance. Accordingly, this enables the safetyneedle assembly to realize the high operability.

Further, in the present invention, preferably the sheath comprises alocking tab inside the opening as a cannula fixing part, the locking tabprotruding from the side wall of the opening to the inside thereof.Herein, the locking tab passes the cannula introduced in the opening,and then fixes the cannula.

This construction enables the cannula housed inside the opening of thesheath to be fixed by a locking tab which is easily molded. Hereby, thecannula fixing part can be produced at low cost.

Further, in the present invention, an attachment part of the sheath iscomprised of cylindrical pins. Herein, the sheath attachment part of thecollar is preferably comprised of protruded ears, including a pair ofthrough halls of respectively housing the cylindrical pins, and insidechamfers of receiving the respective cylindrical pins.

According to the above mentioned construction, the ears of the collarrespectively have the chamfers inside the ears. Hereby, when the sheathis to be attached to the collar, relatively small force is only neededfor attaching the sheath to the collar via the chamfers.

Further, in the present invention, preferably the pair of sheath fixingprotrusions located on the collar respectively has a substantiallytriangle shape and are arranged at the opposite position of the sheathattachment part. Further, preferably the pair of sheath fixingprotrusions has grooves respectively fitting with a pair of wing wallsof the cannula fixing part.

The above mentioned construction enables the pair of sheath fixingprotrusions of the collar to be realized respectively in a simplestructure like a substantially triangle shape having a groove.

EFFECT OF THE INVENTION

According to the present invention, a safety needle assembly having bothhigh safety and operability is provided.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is an exploded perspective view showing the components of asafety needle assembly in a present embodiment.

FIG. 2 is a perspective view of a hub which is a component of a safetyneedle assembly.

FIG. 3A is a perspective view of a collar which is a component of thesafety needle assembly.

FIG. 3B is a perspective view of the collar, as seen from a back side ofthe collar in FIG. 3A.

FIG. 4 is a perspective view of a protector which is a component of thesafety needle assembly.

FIG. 5A is a perspective view of a sheath which is a component of thesafety needle assembly.

FIG. 5B is a perspective view of the sheath as seen from a bottom sideof the sheath in FIG. 5A.

FIG. 6 is a perspective view of the safety needle assembly representinga state that all the components are assembled.

FIG. 7 is a perspective view of the safety needle assembly representinga state ready to be used. This state is prepared by removing a protectorfrom the safety needle assembly in FIG. 6, and exposing a cannula viapivoting the sheath.

FIG. 8 is a perspective view of the safety needle assembly representinga state just before the cannula is to be housed in the sheath. The stateis prepared by pivoting the sheath in the state of the safety needleassembly shown in FIG. 7, after the safety needle assembly has beenused.

FIG. 9A is a perspective view of the safety needle assembly representinga state that the cannula is housed in the sheath. This state is preparedby a user to push a sheath via a finger, the sheath being in the stateof the safety needle assembly shown in FIG. 8.

FIG. 9B is a perspective view of the safety needle assembly as seen froma bottom side of the safety needle assembly in FIG. 9A.

EMBODIMENTS FOR CARRYING OUT THE INVENTION

Hereinafter, embodiments for carrying out the present invention will beexplained in detail referring to the attached drawings (or appropriatelyreferring to the following descriptions besides the drawings).

Here, a safety needle assembly in the present embodiment is used viaconnected with a liquid transfer apparatus such as a syringe(hereinafter, simply called “syringe”). Here, the safety needle assemblyis packaged by blister packaging or the like which is formed byextending a plastic sheet material. In this case, after treating such apackaged product, a user connects the safety needle assembly with asyringe. Alternatively, in the state being connected with a syringe, thesafety needle assembly may be packaged as a product.

First, referring to FIG. 1, the whole construction of the safety needleassembly in the present embodiment will be explained. Note when eachcomponent of the assembly is explained, a “direction” described thereinis defined by the respective directions in FIG. 1, showing “Up” and“Down” , “Front” (or distal end side) and “Back” (or proximal end side),and “Left” and “Right” . In other FIGS, the directions are similarlydescribed to those in FIG. 1. Further, it should be noted that the“proximal end” and the “distal end” may include a peripheral portion ofthe “end” portion instead of only the “end” portion.

The safety needle assembly 100 includes a hub 1, a cannula 2, a collar3, a protector 4 and a sheath 5. Note an assembly having no protector 4is also called a “safety needle assembly 100”, as described hereinafter.

The cannula 2 is connected with the hub 1 in a general method, forexample, using an epoxy resin. The cannula 2 includes a proximal end 21connected with a distal end of the hub 1 and a distal end 22 having ablade surface 20. Note it is preferable to respectively mold the hub 1,the collar 3, the protector 4 and the sheath 5 as one-piece parts.However, the present embodiment is not limited to the above mentionedmethod, and a variety of methods can be applied.

The collar 3 is to be fitted with the hub 1 at a predetermined position.Further, the protector 4 is guided by the hub 1 to be fitted with thecollar 3 and/or the hub 1, thereby to cover the cannula 2 at thefitting. Moreover, the sheath 5 is to be fitted with the collar 3 sothat the sheath 5 can pivot on the collar 3. The detailed explanationswill be described hereinafter.

As shown in FIG. 2, the hub 1 includes a distal end 10 and a proximalend 11 connected with a syringe (not shown in FIG. 2). Here, a throughhole 12 extends along the entire length of the hub 1 in a longitudinaldirection (or front-back direction). The through hole 12 has aperturesat both distal end 10 and proximal end 11 thereof.

A distal end 21 of the cannula 2 in FIG. 1 is fitted and fixed with theinside of the through hole 12 at the distal end 10 of the hub 1 by usingan epoxy resin. Accordingly, a lumen extending along the entire lengthof the cannula 2 is communicated with the through hole 12 inside the hub1.

The distal end 10 of the hub 1 comprises a plurality of ribs 13 in ashape resembling a series of steps, with extending in a longitudinaldirection. The ribs 13 facilitate the collar 3 to be fitted with the hub1 in a coaxial manner (or having central axis “c” be coaxial).

A surface of the hub 1 includes a plurality of protrusions 14 projectingfrom a circumferential outside surface of the hub 1 to an outer sidethereof in a radial direction.

Further, a recessed ring region 15 is located at a distal side of theprotrusions 14. Accordingly, stage parts 16 and 17 neighboring therecessed ring region 15 have larger external diameters than the recessedring region 15.

The proximal end 11 of the hub 1 has a flange 18 projecting to an outerside of the hub 1 in a radial direction. The flange 18 is engaged with,for example, a distal end of a syringe body (not shown). The engagementallows the hub 1 to be connected with the syringe body (not shown). Thisconnection step may be performed by a known method, for example, byengaging the flange 18 with a screw (or female screw) located at adistal end of the syringe body (not shown).

As shown in FIGS. 3A and 3B, the collar 3 has an outline in a circularshape, having a proximal end 38 and a distal end 34. The collar 3further includes a through hole 39 for the attachment to the hub 1.Here, an inside surface of the collar 3 has a plurality of protrusions301 projecting to the internal side. Those protrusions 301 projecting tothe internal side are engaged with the protrusions 14 of the hub 1. Thisengagement enables the collar 3 to be unratatably fixed onto the hub 1.

Further, the collar 3 includes a ring-shaped ridge 302 on an innersurface thereof. The ring-shaped ridge 302 is spread over the wholecircumference at the inner peripheral side of the through hole 39.Hereby, when the collar 3 is attached to the hub 1, the ring-shapedridge 302 is seated onto the recessed ring region 15 of the hub 1.Therefore, the ring-shaped ridge 302 has a smaller internal diameterthan the external diameters of the two stages 16 and 17 directlyneighboring to the recessed ring region 15 of the hub 1. In contrast,the ring-shaped ridge 302 has a substantially equal internal diameter tothe external diameter of the recessed ring region 15 of the hub 1. Notethe ring-shaped ridge 302 projecting to the internal side in the radialdiameter is shown as a consecutive ring-shaped ridge. However, thering-shaped ridge 302 may be formed, as comprised of a plurality ofseparated segments, each of which extends along a part of the innercircumference of the collar 3.

The collar 3 has a pair of ears 31 (or sheath attachment part)projecting to the external side in the radial direction. The upper halfof the ear 31 has a shape formed by halving a substantially cylindricalshape lying on the side. The ear 31 includes an ear hole 33 with acylindrical shape to which a pin 540 of the sheath 5 (as describedhereinafter) is housed, and a chamfer 32. The chamfer 32 is arranged atan upper portion at the internal side of the ear 31, as shown in FIGS.3A and 3B. The pin 540 of the sheath 5 passes along the chamfer 32,thereby to be housed in the ear hole 33.

Namely, a pair of ears 31 enables the sheath 5 to be rotatably attachedto the collar 3. More specifically, the chamfers 32 facilitate a pair ofpins 540 of the sheath 5 to be respectively attached to the pair of ears31 of the collar 3. Further, when the pair of pins 540 is attached tothe pair of ears 31, the pair of ears 31 slightly bends toward theexternal direction so that the ears 31 are estranged each other.Moreover, a thickness of the ear 31 may be appropriately determined byconsidering the strength for resistance to damage, and the flexibilityfor easier attachment of the sheath 5.

The collar 3 includes a ring-shaped ridge 36 projecting to the externalside in the radial direction. The ring-shaped ridge 36 is a componentfor seating the protector 4.

The collar 3 further includes a pair of sheath fixing protrusions 35.The sheath fixing protrusion 35 has a substantially triangle shape, andis arranged at the opposite side of the ear 31. The sheath fixingprotrusion 35 further includes a groove 37 which is to be engaged with awing wall 53 (or cannula fixing part) of the sheath 5.

As shown in FIG. 4, the protector 4 is formed as a hollow member with anelongated cylindrical shape, including a distal end 40 and a proximalend 41. Preferably, the protector 4 is opened at the proximal end 41 andclosed at the distal end 41. A plurality of ribs 42 are arranged in alongitudinal direction at a middle portion of the external surface ofthe protector 4, so that a user can easily hold the protector 4.

The protector 4 is arranged at the position to cover the cannula 2. Thisarrangement allows the protector 4 to cover up the distal end of thecannula 2. At that time, the protector 4 is fixed onto the collar 3and/or the hub 1. Further, the protector 4 can be detachably pivoted soas to expose the distal end 22 of the cannula 2. Note a seating face(not shown) for the collar 3 may be arranged inside the protector 4 atthe proximal end 41 thereof.

As shown in FIGS. 5A and 5B, the sheath 5 includes a proximal end 501and a distal end 521, and is formed as an elongated member in the wholebody. The sheath 5 includes an opening 58 extending along at least aportion of the longitudinal extent of the sheath 5. The opening 58 is aninternal space of the sheath 5. In the present embodiment, the opening58 of the sheath 5 extends along the entire length in the longitudinaldirection. The proximal end 501 is opened in the longitudinal directionof the sheath 5, while the distal end 521 is closed in the longitudinaldirection of the sheath 5.

Further, the sheath 5 includes finger guiding parts 50, 51 and a distalpart 52, which are composed of a pair of side walls and a back wall. Acircular recess 500 is arranged at the back wall of the finger guidingpart 50. The circular recess 500 is used as a finger guiding region towhich a finger of a user operating the sheath 5 contacts.

The back wall of the finger guiding part 51 is formed as a slopedescending to the front portion, in a stepped shape. On the slope,protrusions 510 and recesses 511 are repeatedly arranged so as toincrease the friction against a user's finger.

Further, the back wall of the distal part 52 includes a protrusivestopper 55 which prevents the user's finger of pushing the sheath 5 fromfurther moving toward the distal side of the sheath 5. Also, the backwall of the distal part 52 includes a hole 520 which is formed when alocking tab 57 (or cannula fixing part) is molded. Note the stopper 55is arranged at the vicinity of the center portion in the longitudinaldirection, or at the position closer to the distal end side of thesheath 5, so that a larger moment is generated to smoothly pivot thesheath 5, when a user pushes the sheath 5 by a finger.

The sheath 5 includes a collar connection mechanism 54 (or attachmentpart) having a pair of cylindrical pins 540. The pair of pins 540 is tobe attached to the ear holes 33 of the ears 31 at the collar 3, so as torotatably connect the sheath 5 with the collar 3. Here, each pin 540 ischamfered in order to facilitate the above mentioned connection.

A pair of wing walls 53 is arranged at the proximal end side of thefinger guiding part 50. Inside the wing wall 53, a slope 530 is providedin the direction toward the proximal end 501. The slope 530 allows thesheath 5 to be easily attached to the collar 3 (that is, by relativelysmall force). Further, at the front side of the wing wall 53, isarranged a groove 531 (or cannula fixing part) which fits with thesheath fixing protrusion 35 of the collar 3. Here, it should be notedthat when each sheath fixing protrusion 35 of the collar 3 turns tofitting with the corresponding groove 531, the pair of wing walls 53 isto be expanded outside just before the fitting.

An opening 58 of the sheath 5 has a locking tab 57. The locking tab 57is formed by a punching portion of the back wall of the distal part 52and protrudes inside from the side wall located inside the opening 58.Here, the locking tab 57 is to be bent when the cannula 2 is introducedinto the opening 58. This allows the cannula 2 to move past the side ofthe locking tab 57. Hereby, the locking tab 57 persistently locks thecannula 2 thus moved past the side of the tab 57 by preventing thecannula 2 from moving back. This locking occurs automatically in theabove mentioned movement. In other words, this permanent locking of thecannula 2 fixed inside the sheath 5 can be achieved once the cannula 2has been introduced into the opening 58 thereby to move past the side ofthe locking tab 57. Herein, the rib 56 positions the cannula 2 in theleft-and right direction thereof when the cannula 2 is introduced intothe opening 58.

FIG. 6 shows the safety needle assembly 100 thus assembled by therespective components. As described hereinbefore, the safety needleassembly 100 thus assembled may be packaged in a blister packaging orthe like in the state of FIG. 6, or may be packaged after the assembly100 is connected with a syringe (not shown).

Next, referring to FIGS. 6 and 7, a method for using the safety needleassembly 100 will be explained in case a user exposes the cannula 2 fromthe assembly 100 as shown in FIG. 5.

First, a user pivots the sheath 5 to be apart from the protector 4 so asto remove the protector 4.

After the sheath 5 is pivoted, the user removes the protector 4 andexposes the cannula 2 (see FIG. 7). In this state, the user can use thecannula 2 (for example, to use the cannula 2 for collecting blood from apatient).

Next, referring to FIGS. 7 to 9, a method for using the safety needleassembly 100 will be explained in case a user houses the cannula 2inside the sheath 5 of the assembly 100 in the state of FIG. 7.

First, after a user has finished the usage of the cannula 2, the userpivots the sheath 5 toward the cannula 2 thereby to have the safetyneedle assembly 100 be in the state of FIG. 8.

Then, the user pushes the back wall of the finger guiding part 51 by afinger against the sheath 5. This allows the sheath 5 to be furtherpivoted toward the cannula 2 as shown in FIGS. 9A and 9B. The cannula 2moves past the side of the locking tab 57 to be engaged with the lockingtab 57, and the pair of sheath fixing protrusions 35 of the collar 3 isrespectively engaged with the corresponding grooves 531 of the sheath 5.Hereby, the cannula 2 is locked inside the sheath 5. That is, at thistiming, the cannula 2 is covered by the sheath 5, and further is lockedinside the sheath 5.

As described above, the safety needle assembly 100 in the presentembodiment enables the high safety due to the mechanism thereof (thatis, securing the lower probability that a user erroneously stings thecannula 2 into a body). Further, this also enables the high operabilityto be realized due to the structure thereof that the sheath 5 has thestopper 55 at the vicinity of the central portion in the longitudinaldirection of the sheath 5, or at the position closer to the distal endside than the central portion of the sheath 5. In other words, the abovementioned positioning of the stopper 55 allows a user to push the sheath5 by a user's finger at a distal side from the fulcrum (or at theposition of the pins 540 of the sheath 5), resulting in generation of alarger moment which enables the sheath 5 to be pivoted by relativelysmaller force.

Further, the pair of wing walls 52 each having a slope 530 and a groove531 in the sheath 5 enables the high operability to be realized. Thatis, the wing walls 53 projecting from the body of the sheath 5 are easyto be bent outward, and the slopes 530 facilitate the sheath fixingprotrusions 35 to be introduced of the collar 3 into the grooves 531.Further, the grooves 531 allow the sheath fixing protrusions 35 to befixed therein. Those mechanisms enable the sheath fixing protrusions 35of the collar 3 to be fitted and fixed in the grooves 531 of the wingwalls 53 of the sheath 5 with relatively small force when a user pushesthe sheath 5 by a user's finger.

Moreover, a user can pivot the sheath 5 by pushing not only the slopeprovided with a plurality of protrusions 510 and recesses 511 havinglarge friction but also the circular recess 500 to which a user's fingereasily fits. Accordingly, this allows the high operability to berealized.

Furthermore, the cannula 2 introduced inside the opening 58 of thesheath 5 is locked by the locking tab 57 besides the grooves 531 of thewing walls 53, allowing it less probable that the cannula 2 is exposedafter being housed inside the sheath 5. That is, this makes the safetyhigher. Further, the locking tab 57 is easily molded, allowing thecannula fixing part to be formed at lower cost.

Further, each ear 31 of the collar 3 has a chamfer inside the ear 31,whereby the sheath is attached to the collar 3 through the chamfer,allowing the attachment to need relatively small force.

Further, it is possible to realize that the pair of sheath fixingprotrusions 35 of the collar 3 is formed respectively in a substantiallytriangle having a groove 37, which is made in a simple structure.

Here, the detailed explanations for the embodiments have been completed,while the embodiments of the present invention are not limited to theexamples disclosed hereinbefore.

For example, if there are a plurality of cannulas with differentlengths, different sheaths 5 corresponding to the respective lengths maybe used in the present invention.

Further, a variety of modifications may be appropriately performed withrespect to specific structures without departing from the scope of thepresent invention.

DESCRIPTION OF REFERENCE NUMERALS

1: Hub

2: Cannula

3: Collar

4: Protector

5: Sheath

10: Distal End

11: Proximal End

12: Through Hole

13: Rib

14: Protrusion

15: Recessed Ring Region

16, 17: Stage Part

18: Flange

20: Blade Surface

21: Proximal End

22: Distal End

31: Ear (or Sheath Attachment Part)

32: Chamfer

33: Ear Hole

34: Distal End

35: Sheath Fixing Protrusion

36: Circular Ridge

37: Groove

38: Proximal End

39: Through Hole

40: Distal End

41: Proximal End

42: Rib

50: Finger Guiding Part

51: Finger Guiding Part

52: Distal Part

53: Wing wall (or Cannula Fixing Part)

54: Collar Connection Mechanism (or Attachment Part)

55: Stopper

56: Rib

57: Locking Tab (or Cannula Fixing Part)

58: Opening

100: Safety Needle Assembly

301: Protrusion

302: Ring-shaped Ridge

500: Circular Recess

501: Proximal End

510: Protrusion

511: Recess

520: Hole

521: Distal End

530: Slope

531: Groove (or Cannula Fixing Part)

540: Pin

The invention claimed is:
 1. A safety needle assembly with a sheath,comprising: a hub including a proximal end connecting with a syringe,and a distal end; a cannula including a proximal end connecting with thedistal end of the hub, a lumen extending in a longitudinal direction,and a distal end; a collar attached to the hub, including a sheathattachment part and a pair of sheath fixing protrusions; a protectorcovering the distal end of the cannula by being attached to the hub orthe collar, and being detachable to expose the distal end of thecannula; and an opening partially extending along at least alongitudinal direction of the sheath so as to house the cannula, whereinthe sheath further comprising: a cannula fixing part comprised of a pairof protruding wing walls defining a space therebetween and each of whichis provided with a groove and a sloped portion arranged between thegroove and a proximal end of the sheath, each groove facing the spaceand fitting with a respective sheath fixing protrusion when the cannulais housed in the opening such that the pair of sheath fixing protrusionsis disposed in the space between the pair of protruding wing walls; andan attachment part rotatably supporting the sheath in a direction ofhousing the cannula when the protector is detached to expose the distalend of the cannula, the attachment part being attached to the sheathattachment part of the collar, wherein the pair of protruding wing wallsof the cannula fixing part have projections extending from the slopedportions to partially cover the respective grooves, and the pair ofsheath fixing protrusions of the collar respectively have a triangleshape and are arranged at an opposite position of the sheath attachmentpart, each sheath fixing protrusion of the pair of sheath fixingprotrusions possessing a pair of planar surfaces and a pair of slopedsurfaces which respectively slope down from the pair of planar surfacesto define a channel between said pair of planar surfaces, said channelsrespectively fitting around the projections of the pair of wing walls ofthe cannula fixing part.
 2. The safety needle assembly as described inclaim 1, wherein the attachment part of the sheath is comprised ofcylindrical pins, and the sheath attachment part of the collar iscomprised of protruded ears including a pair of through holes each ofwhich houses the cylindrical pin, and inside chamfers each of whichreceives the cylindrical pin.
 3. The safety needle assembly as describedin claim 1, wherein the wing walls are configured to be bent outward bypushing the sloped portions.
 4. The safety needle assembly as describedin claim 1, wherein each sloped portion has a thickness which decreasesfrom the groove toward the proximal end of the sheath.
 5. The safetyneedle assembly as described in claim 1, wherein the pair of sheathfixing protrusions protrude outwardly from the collar in oppositedirections.